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Tu2008 ASSESSING THE ROLES OF ANTI-TISSUE TRANSGLUTAMINASE IGA AND ANTI-DEAMINATED GLIADIN IGG ANTIBODIES IN DETECTING AND DIAGNOSING PEDIATRIC CELIAC DISEASE

Gastroenterology (New York, N.Y. 1943), 2023-05, Vol.164 (6), p.S-1184-S-1185

2023

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The utility of both anti-deaminated gliadin IgG and anti-tissue transglutaminase IgA antibodies for the diagnosis of coeliac disease without biopsy

Pathology, 2022-03, Vol.54, p.S81-S82

2022

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Implementation of an ex vivo TH17 assay

Pathology, 2017-02, Vol.49, p.S43-S43

2017

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Variability in skin prick test results performed by multiple operators depends on the device used

The World Allergy Organization journal, 2012-12, Vol.5 (12), p.200-204

2012

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Performance of an automated complement ELISA

Pathology, 2018-02, Vol.50, p.S111-S111

2018

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Comparison between staged and synchronous resection for patients with synchronous liver metastases from colon cancer

HPB (Oxford, England), 2020, Vol.22, p.S223-S223

2020

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From pre to post-BMT: autoimmunity and vasculitis in wiskott-aldrich syndrome

Pathology, 2015, Vol.47, p.S39-S39

2015

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Measurement of naive T cells for the diagnosis of severe combined immunodeficiency (SCID)

Pathology, 2014, Vol.46, p.S98-S98

2014

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Interstitial lung disease in common variable immune deficiency

Pathology, 2015, Vol.47, p.S39-S40

2015

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Activating mutations in PIK3CD and murine CD4+ T cells

Journal of allergy and clinical immunology, 2019-02, Vol.144 (1), p.236-253

2019

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MDA-5 associated interstitial lung disease

Pathology, 2016-02, Vol.48, p.S43-S44

2016

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Reply to Comment on: Carboplatin Hypersensitivity Reactions in Pediatric Low Grade Glioma Are Protocol Specific and Desensitization Shows Poor Efficacy

Pediatric blood & cancer, 2016-01, Vol.63 (1), p.175-175

2016

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Reduced Intensity/Reduced Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute Gvhd

Transplantation and cellular therapy, 2021-03, Vol.27 (3), p.S13-S14

2021

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Increasing the accuracy of peanut allergy diagnosis using Ara h2

Pathology, 2013, Vol.45, p.S44-S44

2013

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Evaluation of primary immunodeficiency disorders by flow cytometry

Pathology, 2011, Vol.43, p.S42-S42

2011

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Identification and functional characterization of two novel mutations in the α-helical loop (residues 484-503) of CYBB/gp91(phox) resulting in the rare X91(+) variant of chronic granulomatous disease

Human mutation, 2012-03, Vol.33 (3), p.471-475

2012

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Identification and functional characterization of two novel mutations in the alpha -helical loop (residues 484-503) of CYBB/gp91phox resulting in the rare X91 super(+) variant of chronic granulomatous disease

Human mutation, 2012-03, Vol.33 (3), p.471-475

2012

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Identification and functional characterization of two novel mutations in the α-helical loop (residues 484-503) of CYBB/gp91phox resulting in the rare X91+ variant of chronic granulomatous disease

Human mutation, 2012-03, Vol.33 (3), p.471-475

2012

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Signal transducer and activator of transcription 3 (STAT3) mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8 super(+) T-cell memory formation and function

Journal of allergy and clinical immunology, 2013-08, Vol.132 (2), p.400-411.e9

2013

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STAT3 mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8+ T cell memory formation and function

Journal of allergy and clinical immunology, 2013-07, Vol.132 (2), p.400-11.e9

2013

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Clinical utility of soluble IL-2 receptor alpha in haemophagocytic lymphohistiocytosis

Pathology, 2012, Vol.44, p.S82-S82

2012

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Variability in Skin Prick Test Results Performed by Multiple Operators Depends on the Device Used

The World Allergy Organization journal, 2012-12, Vol.5 (12), p.200-204

2012

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Memory B-cell phenotyping in cvid – a journey through buddha’s nostril?

Pathology, 2011, Vol.43, p.S41-S42

2011

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A case of T-cell-Epstein-Barr virus-haemophagocytic lymphohistiocytosis and sustained remission following ruxolitinib therapy

Clinical & translational immunology, 2023, Vol.12 (7), p.e1459-e1459

2023

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Laboratory Investigations

Textbook of Pediatric Rheumatology, 2016, p.117-128.e6

Seventh Edition, 2016

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Tu2008 ASSESSING THE ROLES OF ANTI-TISSUE TRANSGLUTAMINASE IGA AND ANTI-DEAMINATED GLIADIN IGG ANTIBODIES IN DETECTING AND DIAGNOSING PEDIATRIC CELIAC DISEASE

The utility of both anti-deaminated gliadin IgG and anti-tissue transglutaminase IgA antibodies for the diagnosis of coeliac disease without biopsy

Implementation of an ex vivo TH17 assay

Variability in skin prick test results performed by multiple operators depends on the device used

Performance of an automated complement ELISA

Comparison between staged and synchronous resection for patients with synchronous liver metastases from colon cancer

From pre to post-BMT: autoimmunity and vasculitis in wiskott-aldrich syndrome

Measurement of naive T cells for the diagnosis of severe combined immunodeficiency (SCID)

Interstitial lung disease in common variable immune deficiency

Activating mutations in PIK3CD and murine CD4+ T cells

MDA-5 associated interstitial lung disease

Reply to Comment on: Carboplatin Hypersensitivity Reactions in Pediatric Low Grade Glioma Are Protocol Specific and Desensitization Shows Poor Efficacy

Reduced Intensity/Reduced Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute Gvhd

Increasing the accuracy of peanut allergy diagnosis using Ara h2

Evaluation of primary immunodeficiency disorders by flow cytometry

Identification and functional characterization of two novel mutations in the α-helical loop (residues 484-503) of CYBB/gp91(phox) resulting in the rare X91(+) variant of chronic granulomatous disease

Identification and functional characterization of two novel mutations in the alpha -helical loop (residues 484-503) of CYBB/gp91phox resulting in the rare X91 super(+) variant of chronic granulomatous disease

Identification and functional characterization of two novel mutations in the α-helical loop (residues 484-503) of CYBB/gp91phox resulting in the rare X91+ variant of chronic granulomatous disease

Signal transducer and activator of transcription 3 (STAT3) mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8 super(+) T-cell memory formation and function

STAT3 mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8+ T cell memory formation and function

Clinical utility of soluble IL-2 receptor alpha in haemophagocytic lymphohistiocytosis

Variability in Skin Prick Test Results Performed by Multiple Operators Depends on the Device Used

Memory B-cell phenotyping in cvid – a journey through buddha’s nostril?

A case of T-cell-Epstein-Barr virus-haemophagocytic lymphohistiocytosis and sustained remission following ruxolitinib therapy

Laboratory Investigations

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